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TAPERFILL HIP Adverse Event — Injury (MDR 1644408-2020-00357)

TAPERFILL HIP Adverse Event — Injury (MDR 1644408-2020-00357) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: TAPERFILL HIP; Generic name: TAPERFILL HIP STEM, STANDARD, SIZE 12; Manufacturer: ENCORE MEDICAL L.P..

DeviceTAPERFILL HIP
Generic nameTAPERFILL HIP STEM, STANDARD, SIZE 12
ManufacturerENCORE MEDICAL L.P.
Report number1644408-2020-00357
Event typeInjury
Product problemN
Date received2020-04-28
Report sourceCOMPANY REPRESENTATIVE
NarrativeTHE REASON FOR THIS REVISION SURGERY WAS REPORTED AS A MICRO FRACTURE. THE PREVIOUS SURGERY AND THE SURGERY DETAILED IN THIS EVENT OCCURRED 3.7 MONTHS APART. THE HEALTHCARE PROFESSIONAL INDICATED THERE WAS NO DELAY IN SURGERY AND ANOTHER SUITABLE DEVICE WAS AVAILABLE FOR USE. THE REVISION SURGERY WAS COMPLETED AS INTENDED. THE DEVICES WERE DISPOSED OF AT HOSPITAL AND NOT MADE AVAILABLE TO DJO SURG
SourceopenFDA MAUDE (device adverse events)

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